A dual-purpose copper(I) coordination polymer for the construction of self-driven photoinduced C-H arylation systems

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Yue Zhang, Ying-Ying Zhang, Shuo Li, Fei Wang, Yuanmeng Tao, Jiaxing Cui, Chao Huang, Liwei Mi
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引用次数: 0

Abstract

The simultaneous exploitation of dual or multiple physical and chemical properties of a material is a promising strategy for developing high-tech intelligent complex systems. In this study, a copper(I) coordination polymer (CuI-CP, 2) was synthesized and utilized as a dual-purpose material to construct a self-powered photocatalytic system capable of significantly improving the power generation capabilities of triboelectric generators (TEGs) as a triboelectric layer and efficiently catalyzing the C-H arylation reaction as a photocatalyst. Compound 2 was achieved via a solvothermal method in the presence of ammonia and ethylenediamine. In contrast, only mixed-valence cooper salts ([CuII(H2O)5][CuI3(CN)5]·H2O, 1) were obtained without ammonia and ethylenediamine. Comparative analysis revealed that TEG based on 2 (2-TEG) showcased superior output performance compared to 1-TEG owing to the exceptional electron-donating ability of 2. Furthermore, under light-emitting diodes (LEDs) irradiation powered by 2-TEG, 2 demonstrated remarkable catalytic activity and selectivity in the photoinduced C-H arylation of benzothiazole, far exceeding the performance of 1. This research highlights the potential of bifunctional material 2 with a distinctive structure, renowned for its outstanding energy harvesting and conversion capabilities as well as excellent photocatalytic performance, thereby facilitating the design objectives of multitasking in self-driven complex systems.
用于构建自驱动光诱导 C-H 芳基化体系的两用铜(I)配位聚合物
同时利用材料的双重或多重物理和化学特性,是开发高科技智能复合系统的一种前景广阔的策略。本研究合成了一种铜(I)配位聚合物(CuI-CP,2),并将其作为一种两用材料来构建自供电光催化系统,该系统既能作为三电层显著提高三电发电机(TEG)的发电能力,又能作为光催化剂高效催化 C-H 芳基化反应。化合物 2 是在氨和乙二胺存在下通过溶热法制得的。相反,在没有氨和乙二胺的情况下,只得到了混合价配合盐([CuII(H2O)5][CuI3(CN)5]-H2O, 1)。对比分析表明,基于 2 的 TEG(2-TEG)的输出性能优于 1-TEG,这是由于 2 具有优异的电子负载能力。此外,在 2-TEG 驱动的发光二极管(LED)照射下,2 在光诱导苯并噻唑的 C-H 芳基化过程中表现出显著的催化活性和选择性,远远超过了 1 的性能。这项研究凸显了具有独特结构的双功能材料 2 的潜力,这种材料以其出色的能量收集和转换能力以及优异的光催化性能而闻名,从而促进了在自驱动复杂系统中实现多重任务的设计目标。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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